ITMI20061492A1 - Processo per la preparazione di fexofenadina. - Google Patents
Processo per la preparazione di fexofenadina. Download PDFInfo
- Publication number
- ITMI20061492A1 ITMI20061492A1 IT001492A ITMI20061492A ITMI20061492A1 IT MI20061492 A1 ITMI20061492 A1 IT MI20061492A1 IT 001492 A IT001492 A IT 001492A IT MI20061492 A ITMI20061492 A IT MI20061492A IT MI20061492 A1 ITMI20061492 A1 IT MI20061492A1
- Authority
- IT
- Italy
- Prior art keywords
- process according
- organic solvent
- fexofenadine
- compound
- hydrogenation
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 23
- 238000002360 preparation method Methods 0.000 title claims description 5
- 229960003592 fexofenadine Drugs 0.000 claims abstract description 18
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims abstract description 17
- -1 carboxylate salt Chemical class 0.000 claims abstract description 15
- 239000003960 organic solvent Substances 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims abstract description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000003054 catalyst Substances 0.000 claims abstract description 10
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 10
- 230000007062 hydrolysis Effects 0.000 claims abstract description 7
- 238000006460 hydrolysis reaction Methods 0.000 claims abstract description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical group [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- 229910052763 palladium Inorganic materials 0.000 claims description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 5
- 150000001768 cations Chemical class 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 2
- 238000009835 boiling Methods 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 229910052697 platinum Inorganic materials 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000003495 polar organic solvent Substances 0.000 claims 1
- 150000007942 carboxylates Chemical class 0.000 abstract description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 2
- 239000001257 hydrogen Substances 0.000 abstract description 2
- 238000006386 neutralization reaction Methods 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 12
- 150000002148 esters Chemical class 0.000 description 6
- 238000010992 reflux Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- YFKBXYGUSOXJGS-UHFFFAOYSA-N 1,3-Diphenyl-2-propanone Chemical compound C=1C=CC=CC=1CC(=O)CC1=CC=CC=C1 YFKBXYGUSOXJGS-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 238000007327 hydrogenolysis reaction Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000010531 catalytic reduction reaction Methods 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/20—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
- C07D211/22—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Hydrogenated Pyridines (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Saccharide Compounds (AREA)
- Compounds Of Iron (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT001492A ITMI20061492A1 (it) | 2006-07-27 | 2006-07-27 | Processo per la preparazione di fexofenadina. |
| DE602007010638T DE602007010638D1 (de) | 2006-07-27 | 2007-07-25 | Verfahren zur herstellung von fexofenadin |
| KR1020097001409A KR101413877B1 (ko) | 2006-07-27 | 2007-07-25 | 펙소페나딘의 제조 방법 |
| EP07805737A EP2046743B1 (en) | 2006-07-27 | 2007-07-25 | Process for preparing fexofenadine |
| US12/374,539 US9403770B2 (en) | 2006-07-27 | 2007-07-25 | Process for preparing fexofenadine |
| ES07805737T ES2356269T3 (es) | 2006-07-27 | 2007-07-25 | Procedimiento para preparar fexofenadina. |
| AT07805737T ATE488502T1 (de) | 2006-07-27 | 2007-07-25 | Verfahren zur herstellung von fexofenadin |
| PCT/IT2007/000525 WO2008012858A1 (en) | 2006-07-27 | 2007-07-25 | Process for preparing fexofenadine |
| CN2007800276927A CN101522619B (zh) | 2006-07-27 | 2007-07-25 | 非索非那定的制备方法 |
| JP2009521422A JP5196501B2 (ja) | 2006-07-27 | 2007-07-25 | フェキソフェナジンの調製方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT001492A ITMI20061492A1 (it) | 2006-07-27 | 2006-07-27 | Processo per la preparazione di fexofenadina. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ITMI20061492A1 true ITMI20061492A1 (it) | 2008-01-28 |
Family
ID=38777957
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IT001492A ITMI20061492A1 (it) | 2006-07-27 | 2006-07-27 | Processo per la preparazione di fexofenadina. |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US9403770B2 (ko) |
| EP (1) | EP2046743B1 (ko) |
| JP (1) | JP5196501B2 (ko) |
| KR (1) | KR101413877B1 (ko) |
| CN (1) | CN101522619B (ko) |
| AT (1) | ATE488502T1 (ko) |
| DE (1) | DE602007010638D1 (ko) |
| ES (1) | ES2356269T3 (ko) |
| IT (1) | ITMI20061492A1 (ko) |
| WO (1) | WO2008012858A1 (ko) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106699559B (zh) * | 2015-11-12 | 2021-04-06 | 浙江九洲药业股份有限公司 | 一种洛索洛芬钠的制备工艺 |
| CN107782804B (zh) * | 2016-08-25 | 2020-11-13 | 人福普克药业（武汉）有限公司 | 检测盐酸非索非那定样品中有关物质的方法 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4254130A (en) * | 1979-04-10 | 1981-03-03 | Richardson-Merrell Inc. | Piperidine derivatives |
| US4254129A (en) * | 1979-04-10 | 1981-03-03 | Richardson-Merrell Inc. | Piperidine derivatives |
| US5136070A (en) * | 1991-12-23 | 1992-08-04 | Dow Corning Corporation | Sodium borohydride catalyzed disproportionation of cycloorganosilanes |
| WO1993021156A1 (en) * | 1992-04-10 | 1993-10-28 | Merrell Dow Pharmaceuticals Inc. | 4-diphenylmethyl piperidine derivatives and process for their preparation |
| DE69415319T2 (de) * | 1993-06-24 | 1999-06-10 | Albany Molecular Research, Inc., Albany, N.Y. | Verfahren zur herstellung von piperidinderivaten |
| US20020007068A1 (en) * | 1999-07-16 | 2002-01-17 | D'ambra Thomas E. | Piperidine derivatives and process for their production |
| ATE230395T1 (de) | 1993-06-25 | 2003-01-15 | Merrell Pharma Inc | Neue zwischenprodukte für die herstellung von antihistaminschen 4- diphenylmethyl/diphenylmethoxypiperidin-derivat n |
| US6153754A (en) * | 1995-12-21 | 2000-11-28 | Albany Molecular Research, Inc. | Process for production of piperidine derivatives |
| US6201124B1 (en) * | 1995-12-21 | 2001-03-13 | Albany Molecular Research, Inc. | Process for production of piperidine derivatives |
| US6689898B2 (en) | 1998-07-02 | 2004-02-10 | Aventis Pharmaceuticals Inc. | Antihistaminic piperidine derivatives and intermediates for the preparation thereof |
| ITRM20010260A1 (it) * | 2001-05-17 | 2002-11-18 | Dinamite Dipharma S P A In For | Processo per la preparazione della fexofenadina o acido 4 1-idrossi-4-4- (idrossidifenilmetil)-1-piperidinil|-butil|-alfa,alfa-dimetilbenz |
| US6743941B2 (en) | 2001-06-15 | 2004-06-01 | Aventis Pharma Deutschland Gmbh | Process for the production of piperidine derivatives |
| ITMI20041143A1 (it) * | 2004-06-08 | 2004-09-08 | Dipharma Spa | Polimorfi di fexofenadina e procedimento per la loro preparazione |
| US20060148851A1 (en) * | 2004-09-28 | 2006-07-06 | Shlomit Wizel | Fexofenadine crystal form and processes for its preparation thereof |
-
2006
- 2006-07-27 IT IT001492A patent/ITMI20061492A1/it unknown
-
2007
- 2007-07-25 CN CN2007800276927A patent/CN101522619B/zh not_active Expired - Fee Related
- 2007-07-25 DE DE602007010638T patent/DE602007010638D1/de active Active
- 2007-07-25 WO PCT/IT2007/000525 patent/WO2008012858A1/en active Application Filing
- 2007-07-25 ES ES07805737T patent/ES2356269T3/es active Active
- 2007-07-25 AT AT07805737T patent/ATE488502T1/de not_active IP Right Cessation
- 2007-07-25 US US12/374,539 patent/US9403770B2/en not_active Expired - Fee Related
- 2007-07-25 JP JP2009521422A patent/JP5196501B2/ja not_active Expired - Fee Related
- 2007-07-25 KR KR1020097001409A patent/KR101413877B1/ko not_active IP Right Cessation
- 2007-07-25 EP EP07805737A patent/EP2046743B1/en not_active Not-in-force
Also Published As
| Publication number | Publication date |
|---|---|
| KR20090034905A (ko) | 2009-04-08 |
| ES2356269T3 (es) | 2011-04-06 |
| JP2009544691A (ja) | 2009-12-17 |
| EP2046743B1 (en) | 2010-11-17 |
| CN101522619B (zh) | 2012-01-04 |
| WO2008012858A1 (en) | 2008-01-31 |
| ATE488502T1 (de) | 2010-12-15 |
| DE602007010638D1 (de) | 2010-12-30 |
| US9403770B2 (en) | 2016-08-02 |
| KR101413877B1 (ko) | 2014-06-30 |
| CN101522619A (zh) | 2009-09-02 |
| US20110190504A1 (en) | 2011-08-04 |
| EP2046743A1 (en) | 2009-04-15 |
| JP5196501B2 (ja) | 2013-05-15 |
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